QM/MM modeling of class A β-lactamases reveals distinct acylation pathways for ampicillin and cefalexin. Issue 42 (14th October 2021)

• Record Type: Journal Article
• Authors: Song, Zilin; Trozzi, Francesco; Palzkill, Timothy; Tao, Peng
• Is Part Of: Organic & biomolecular chemistry. Volume 19:Issue 42(2021)
• Page Start: 9182
• Page End: 9189
• Publication Date: 2021-10-14
• Subjects: Chemistry, Organic -- Periodicals; Bioorganic chemistry -- Periodicals; Chemistry, Physical organic -- Periodicals; 547
• DOI: 10.1039/d1ob01593a
• Languages: English
• ISSNs: 1477-0520

Abstract

Abstract : QM/MM chain-of-states calculations of CTX-M-44 show distinct acylation profiles for ampicillin and cefalexin, the acylation resistance observed for cefalexin attributes to decreased proton affinity induced by the delocalized π-conjugation. Abstract : Efficient mechanism-based design of antibiotics that are not susceptible to β-lactamases is hindered by the lack of comprehensive knowledge on the energetic landscapes for the hydrolysis of various β-lactams. Herein, we adopted efficient quantum mechanics/molecular mechanics simulations to explore the acylation reaction catalyzed by CTX-M-44 (Toho-1) β-lactamase. We show that the catalytic pathways for β-lactam hydrolysis are correlated to substrate scaffolds: using Glu166 as the only general base for acylation is viable for ampicillin but prohibitive for cefalexin. The present computational workflow provides quantitative insights to facilitate the optimization of future β-lactam antibiotics.